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Renal and prostate stones composition in alkaptonuria: a case report
- Source :
- Clinical Nephrology. 84:339-342
- Publication Year :
- 2015
- Publisher :
- Dustri-Verlgag Dr. Karl Feistle, 2015.
-
Abstract
- Alkaptonuria is a genetic disorder characterized by an accumulation of homogentisic acid due to an enzymatic defect of homogentisate 1,2 dioxygenase. The homogentisic acid is excreted exclusively by both glomerular filtration and tubular secretion leading to the renal parenchyma being exposed to high concentrations of homogentisic acid. The alkaptonuric patients are at higher risk of renal stones (and of prostate stones for males), usually in the later stages of the disease. We describe the case of a 51-year-old man whose renal and prostate stones were analyzed by X-ray diffraction and infrared spectroscopy, respectively. We review the cases of alkaptonuria (AKU) patients reported in the literature for whom the composition of kidney or prostate stones was assessed with physical or chemical techniques. In this paper, we also discuss the advantages and drawbacks of the different methodologies.
- Subjects :
- Calcium Phosphates
Male
Prostatic Diseases
medicine.medical_specialty
Spectrophotometry, Infrared
Calcium oxalate
Urology
Renal function
Alkaptonuria
Calculi
Kidney Calculi
chemistry.chemical_compound
X-Ray Diffraction
Apatites
Internal medicine
medicine
Humans
Homogentisic acid
Homogentisic Acid
Homogentisate 1,2-dioxygenase
Kidney
Calcium Oxalate
business.industry
Genetic disorder
General Medicine
Middle Aged
medicine.disease
Endocrinology
medicine.anatomical_structure
chemistry
Nephrology
business
Subjects
Details
- ISSN :
- 03010430
- Volume :
- 84
- Database :
- OpenAIRE
- Journal :
- Clinical Nephrology
- Accession number :
- edsair.doi.dedup.....337cc06255c78258ef4db5c9626779d4
- Full Text :
- https://doi.org/10.5414/cn108608